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用于胚胎干细胞的量子点成像。

Quantum dot imaging for embryonic stem cells.

作者信息

Lin Shuan, Xie Xiaoyan, Patel Manishkumar R, Yang Yao-Hung, Li Zongjin, Cao Feng, Gheysens Oliver, Zhang Yan, Gambhir Sanjiv S, Rao Jiang Hong, Wu Joseph C

机构信息

Molecular Imaging Program at Stanford (MIPS) and Bio-X Program, Department of Radiology, Stanford University, Stanford, CA 94305, USA.

出版信息

BMC Biotechnol. 2007 Oct 9;7:67. doi: 10.1186/1472-6750-7-67.

Abstract

BACKGROUND

Semiconductor quantum dots (QDs) hold increasing potential for cellular imaging both in vitro and in vivo. In this report, we aimed to evaluate in vivo multiplex imaging of mouse embryonic stem (ES) cells labeled with Qtracker delivered quantum dots (QDs).

RESULTS

Murine embryonic stem (ES) cells were labeled with six different QDs using Qtracker. ES cell viability, proliferation, and differentiation were not adversely affected by QDs compared with non-labeled control cells (P = NS). Afterward, labeled ES cells were injected subcutaneously onto the backs of athymic nude mice. These labeled ES cells could be imaged with good contrast with one single excitation wavelength. With the same excitation wavelength, the signal intensity, defined as (total signal-background)/exposure time in millisecond was 11 +/- 2 for cells labeled with QD 525, 12 +/- 9 for QD 565, 176 +/- 81 for QD 605, 176 +/- 136 for QD 655, 167 +/- 104 for QD 705, and 1,713 +/- 482 for QD 800. Finally, we have shown that QD 800 offers greater fluorescent intensity than the other QDs tested.

CONCLUSION

In summary, this is the first demonstration of in vivo multiplex imaging of mouse ES cells labeled QDs. Upon further improvements, QDs will have a greater potential for tracking stem cells within deep tissues. These results provide a promising tool for imaging stem cell therapy non-invasively in vivo.

摘要

背景

半导体量子点(QDs)在体外和体内细胞成像方面的潜力与日俱增。在本报告中,我们旨在评估用Qtracker递送的量子点(QDs)标记的小鼠胚胎干细胞(ES)的体内多重成像。

结果

使用Qtracker用六种不同的量子点标记小鼠胚胎干细胞(ES)。与未标记的对照细胞相比,量子点对ES细胞的活力、增殖和分化没有不利影响(P =无显著性差异)。之后,将标记的ES细胞皮下注射到无胸腺裸鼠的背部。这些标记的ES细胞可以在单一激发波长下以良好的对比度成像。在相同的激发波长下,信号强度定义为(总信号-背景)/曝光时间(毫秒),对于用QD 525标记的细胞为11±2,对于QD 565为12±9,对于QD 605为176±81,对于QD 655为176±136,对于QD 705为167±104,对于QD 800为1713±482。最后,我们表明QD 800比其他测试的量子点具有更高的荧光强度。

结论

总之,这是首次对用QDs标记的小鼠ES细胞进行体内多重成像的证明。经过进一步改进,量子点在追踪深部组织中的干细胞方面将具有更大的潜力。这些结果为在体内非侵入性地成像干细胞治疗提供了一个有前景的工具。

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